Hong Jun Young, Zhang Xiaoyu, Lin Hening
Department of Chemistry and Chemical Biology, Cornell University, Ithaca, NY, USA.
Department of Chemistry and Chemical Biology, Howard Hughes Medical Institute, Cornell University, Ithaca, NY, USA.
Methods Mol Biol. 2018;1813:225-234. doi: 10.1007/978-1-4939-8588-3_15.
Sirtuins are a class of enzymes that utilize nicotinamide adenine dinucleotide, NAD, to remove various acyl groups from protein lysine residues. They have important biological functions and regulate numerous biological pathways. Small molecules that can modulate sirtuin enzymatic activities are potential therapeutic candidates to treat various human diseases. This protocol describes a high-performance liquid chromatography (HPLC)-based method to measure the enzyme kinetics for SIRT2 and SIRT6's demyristoylase activities and SIRT5's desuccinylase activity. This method uses peptide substrates that resemble physiological substrates and thus can give more reliable kinetic parameters (K and k values) for these enzymes. The data obtained are useful for understanding the biological function of sirtuins and developing sirtuin modulators.
沉默调节蛋白是一类利用烟酰胺腺嘌呤二核苷酸(NAD)从蛋白质赖氨酸残基上去除各种酰基的酶。它们具有重要的生物学功能,并调节众多生物学途径。能够调节沉默调节蛋白酶活性的小分子是治疗各种人类疾病的潜在候选药物。本方案描述了一种基于高效液相色谱(HPLC)的方法,用于测量SIRT2和SIRT6的脱肉豆蔻酰酶活性以及SIRT5的去琥珀酰化酶活性的酶动力学。该方法使用类似于生理底物的肽底物,因此可以为这些酶提供更可靠的动力学参数(K和k值)。所获得的数据对于理解沉默调节蛋白的生物学功能和开发沉默调节蛋白调节剂很有用。